In this role, you will have the opportunity to:
Interact with various teams across the globe to understand the requirements.
Plan, develop, execute tests and track test activities, adhering to timeline and quality.
Participates in discussions and reviews of test plans, test procedures and software requirements.
Develop and execute both automated and manual test cases based on analyzed requirements and overall test strategy.
Report errors in bug tracking tool and track the issues to closure incl. support of defect investigation, validate defect fixes and analyze impact of fixes.
Develop, maintain and communicate status of the project.
Collaborate with software development team, the functional manager, project manager, distributed, cross-functional teams to ensure products meet quality, performance, scalability, and reliability and schedule goals.
Prepare appropriate documentation as required by internal product development processes and regulatory agencies.
The essential requirements of the job include
Bachelor’s degree in Computer Science, Software Engineering or a related field with 2-6 years of experience.
Experience in developing medical device software and working knowledge of FDA Quality Systems Regulation is desirable.
Requires proven experience in software testing.
Experience in developing manual test cases.
Experience with Visual Studio 2012 or later.
Experience with Windows operating systems.
Test scripting.
Experience in requirement gathering and deducing test scenarios.
Experience with Azure Devops.
Experience with a Test Management Tool.
It would be a plus if you also possess previous experience in:
Experience in medical device design & development in Agile environment is a plus.
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